US4118528A - Glass fiber friction facing - Google Patents

Glass fiber friction facing Download PDF

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Publication number
US4118528A
US4118528A US05/819,760 US81976077A US4118528A US 4118528 A US4118528 A US 4118528A US 81976077 A US81976077 A US 81976077A US 4118528 A US4118528 A US 4118528A
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United States
Prior art keywords
percent
rovings
tape
weight
impregnated
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Expired - Lifetime
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US05/819,760
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English (en)
Inventor
Blaine E. Lowry
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Raymark Industries Inc
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Raybestos Manhattan Inc
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Publication date
Application filed by Raybestos Manhattan Inc filed Critical Raybestos Manhattan Inc
Priority to US05/819,760 priority Critical patent/US4118528A/en
Priority to CA306,621A priority patent/CA1077868A/fr
Priority to IT50408/78A priority patent/IT1107786B/it
Priority to SE7808041A priority patent/SE425168B/sv
Priority to JP53090538A priority patent/JPS5945005B2/ja
Priority to GB7831326A priority patent/GB2002466B/en
Priority to BE189524A priority patent/BE869305A/fr
Priority to FR7822327A priority patent/FR2398771A1/fr
Priority to DE2833289A priority patent/DE2833289C2/de
Application granted granted Critical
Publication of US4118528A publication Critical patent/US4118528A/en
Assigned to RAYMARK INDUSTRIES, INC. reassignment RAYMARK INDUSTRIES, INC. MERGER (SEE DOCUMENT FOR DETAILS). Assignors: RAYBESTOS-MANHATTAN, INC., A CT CORP.
Assigned to FIDELCOR BUSINESS CREDIT CORPORATION reassignment FIDELCOR BUSINESS CREDIT CORPORATION SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: RAYMARK INDUSTRIES, INC.
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D69/00—Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
    • F16D69/02—Composition of linings ; Methods of manufacturing
    • F16D69/025—Compositions based on an organic binder
    • F16D69/026—Compositions based on an organic binder containing fibres
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/21—Circular sheet or circular blank
    • Y10T428/213—Frictional
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof

Definitions

  • the present invention relates to friction elements such as clutch facings and the method of making such elements using rovings of continuous glass fibers as both the reinforcing and friction material.
  • Friction elements such as automotive clutch facings, are subjected to high rotational and high centrifugal forces which have been known to cause the friction elements to burst.
  • friction elements particularly clutch facings, capable of withstanding the hot burst test at rotational speeds in excess of 12,500 rpm and even as high as 14,500 rpm, while maintaining the same physical dimensions, can be formed from bundles of continuous glass fibers wound randomly upon themselves, provided that said fibers are impregnated with a pre-coat composition comprising rubber, resin and furnace black prior to application of a heat-curable cement system comprising rubber, resin and friction modifiers.
  • FIG. 1 represents a tape formed of continuous glass fibers impregnated with the heat-curable cement system of this invention wound upon itself into disc-like form.
  • FIG. 2 shows a clutch facing of glass fiber tape impregnated with the heat-curable cement system in three stages of its formation.
  • FIG. 3 is an elevation or face view of a clutch facing according to this invention.
  • FIG. 4 is a side or edge view of the clutch facing shown in FIG. 3.
  • the reference numeral 10 indicates an annularly shaped disc-like friction element such as a clutch facing.
  • the clutch facing is formed by wrapping continuous bundle or tape 12 of generally continuous glass filaments impregnated with the heat-curable cement system in undulating fashion, as shown in FIGS. 1 and 2, to form a disc-like preform which is then consolidated and the cement system is cured by application of heat and pressure.
  • FIG. 1 shows schematically the method by which continuous tape 12 is wound in undulating manner onto a revolving mandrel 20, whereby the tape constantly varies in the instantaneous radius at which it is being wound.
  • the clutch facing 10 is shown as having three segments I, II and III, which segments illustrate the complete clutch facing (I), and the intermediate (II) and early (III) stages of formation of the preform.
  • the tape 12 is formed by combining a plurality of, generally 5 to 10, and preferably 6 to 8, bundles or rovings of continuous glass filaments or fibers.
  • a “filament” or “fiber” of glass is meant to define a substantially continuous individual fiber of glass having a considerable uninterrupted length, e.g. several thousand feet.
  • a “roving” refers to a collection or assembly of a great number of substantially parallel individual glass filaments.
  • a roving may include from 100 up to 2000, preferably 1500 to 2000 individual filaments gathered together in any manner well known in the art and technology of glass fiber manufacture.
  • the rovings ordinarily will be free of twist, but may have a relatively small amount of twist not exceeding about one turn per foot.
  • the filaments of which the rovings are formed are extremely fine having diameters ranging from about 10 to 15 microns. Preferably the diameter of the filaments is on the order of 12 to 14 microns.
  • the glass filaments be first treated in such manner as to enable them to form a strong and permanent bond with the below described pre-coat. This can be accomplished by application of one or more anchoring agents to the filaments just after they are formed.
  • a suitable anchoring agent is represented by the amino silanes such as gamma-aminopropyltriethoxy silane or by a smilar silane having a carboxyl group in the organic group attached to the silicon atom or an amino or carboxyl group in the carboxylato group of a coordination compound. These may be applied to the glass filament surfaces or incorporated as a component of a size composition.
  • the use of such silanes as anchoring agents is disclosed in U.S. Pat. No. 3,287,204 issued Nov. 22, 1966.
  • Another treatment to obtain enhanced bonding of the pre-coat to glass filaments involves the application thereto of an aqueous solution of magnesium chloride, zinc chloride, or magnesium hydroxide or zinc hydroxide.
  • the solution in aqueous medium may be adjusted to an alkaline pH to effect deposition on the glass filaments in the form of the hydroxide.
  • the hydroxides are then converted to the corresponding oxides by heat treatment. This method is described in U.S. Pat. No. 3,311,528 issued Mar. 28, 1967.
  • the glass filaments or fibers may also be rendered receptive to forming a strong bond with the pre-coat by treating the glass fibers with a size having as an essential ingredient, the reaction product of an imidazoline having a long chain fatty acid group containing at least 5 carbon atoms and an unsaturated polyester resin formed in an uncured state as disclosed in U.S. Pat. No. 3,097,963 issued July 16, 1963.
  • This invention is not limited to any specific treatment of the glass filaments, provided the treatment provides the glass filament surfaces with the ability to form a strong bond with the pre-coat.
  • the pre-coat with which the glass fiber rovings are impregnated contains as essential constituents a vulcanizable carboxy nitrile rubber; a water-soluble, one-step, thermosetting phenol formaldehyde resin, and furnace black, in specified proportions.
  • the pre-coat is applied in the form of an aqueous dispersion which also contains a surfactant.
  • the vulcanizable carboxy nitrile rubber is a high strength, oil resistant rubber composed of at least three monomers, namely, acrylonitrile, butadiene and one or more acrylic-type acids.
  • the copolymerization of these monomers produces a chain similar to a normal nitrile rubber except for the carboxyl groups which are distributed along the chain with a frequence of about 1 to every 100 to 200 carbon atoms.
  • This type polymer is unique in that it can be cured or vulcanized by reactions of the carboxylic group as well as normal sulfur-type vulcanization.
  • One method of curing is to crosslink the chains by neutralizing the carboxylic groups with the oxide or salt of polyvalent metal.
  • the Ca ++ , Mg ++ , and Pb ++ ions are capable of effecting such a vulcanization reaction.
  • the polymer chains also contain double bonds such as occur in butadiene-acrylonitrile rubbers, the normal types of sulfur vulcanization can also be employed.
  • the metal oxide and sulfur-curing systems are applicable to both the dry rubber and latex form of the carboxylated nitrile rubbers.
  • the carboxy modification exhibits much higher tensile strength and modulus, lower elongation, higher hardness, much improved hot tear and tensile, better low-temperature brittleness, improved ozone resistance, and better retention of physical properties after hot-oil and air aging.
  • the carboxy nitrile rubber is available in the form of a latex which is stable over a pH range of 3.5 to 9.5.
  • the latex can be cured by means of conventional curing systems such as sulfur, metal oxide and accelerator, or by use of metal oxide alone. In the latex case, 5 to 10 parts per 100 of polymer solids are generally needed.
  • the heat-curable cement system contains a water-soluble, one-step, thermosetting phenol formaldehyde resin.
  • This resin prior to curing, comprises a mixture of phenols reacted with one or more molecules of aldehyde to form compounds such as ##STR1## Such resin, cures in one to two minutes on a hot plate at temperatures on the order of about 265-285° F.
  • both the pre-coat and heat-curable cement systems are applied to the glass filaments in the form of aqueous dispersions, thereby obviating the potential fire and ecological problems presented by the use of organic solvents and making possible reduction in processing costs.
  • the improved hot burst strengths obtainable according to this invention are attributable, at least in part, to the use of such aqueous systems. It is believed application of the pre-coat to the glass filaments in the form of an aqueous dispersion may make possible the better wetting of the filaments by the pre-coat by reason of the presence of certain type furnace black and of various surfactants and/or dispersion aids in the dispersions.
  • aqueous dispersion of the pre-coat used in this invention contains as an essential constituent furnace black having a finite particle size in the range of about 65 to about 85 m ⁇ .
  • furnace black is one of low color having an average particle size of about 75 m ⁇ , supplied as an anionic dispersion of 50% solids, and having a density of about 10.8 lbs./gal. Applicant believes that the furnace black having the above designated particle size performs the very important function of aiding the rubber and resin constituents of the pre-coat to wet the glass filaments, whereby the hot burst strength of the ultimate clutch facings is considerably enhanced.
  • the surfactants preferably are of the non-ionic type, exemplary of which is octyl phenoxy polyethoxy ethanol.
  • Representative of useful dispersants are sodium lignin sulfonates and sodium salts of carboxylated polyelectrolytes. These surfactants and dispersants generally may be present in the dispersions in amounts from about 0.25 to about 1.25 percent, by weight, based on the total weight of pre-coat solids.
  • the pre-coat dispersions may also contain small but effective amounts of various suspending aids such as polyacrylates, sodium carboxymethylcellulose gums and acicular-shaped magnesium aluminum silicate particles.
  • the pre-coat is applied first to the glass filaments followed by application of the heat-curable cement system.
  • a relatively low solids aqueous dispersion i.e. one having a solids content of about 10 to 15 percent, preferably 11 to 12 percent.
  • a relatively high solids aqueous dispersion is employed, during which latter step the major portion of the binder including friction modifiers is applied to the filaments.
  • the pre-coating step it is important that the bundles of filaments be opened up or splayed, to provide an opportunity for the pre-coat dispersion to penetrate into the fiber bundle more easily so that all filaments are contacted by the dispersion and pick-up pre-coat solids along their length.
  • the strands or rovings may be passed through a comb-like device before they enter the coater, which generally is of the roller type, whereby the fiber bundles are opened up for intimate contact with the coating composition.
  • the aqueous dispersion should contain on the order of about 40 to about 50 percent, by weight, of carboxy nitrile rubber, about 40 to 50 percent phenol formaldehyde resin, and about 10 to 20 percent furnace black, said percentages being by weight based on the total weight of cement solids.
  • the dispersion contains about 40 to 45 percent of each of the rubber and resin and about 10 to 15 percent of furnace black.
  • the dispersion should also contain a small amount of a surfactant or dispersant as noted above.
  • the bundles of glass filaments are dried to a moisture content on the order of about 2 to 4 percent, by weight of coated filaments.
  • the fiber bundles from the pre-coating step after being dried to the above described extent, will be coated by about 8 to 12 percent, preferably about 10 percent, by weight, based on the weight of uncoated fibers, of pre-coat solids.
  • the heat-curable cement system Following the pre-coating operation as described herein above, there is applied to the fiber glass rovings the heat-curable cement system.
  • This system is applied as a high solids aqueous dispersion, and generally will comprise from about 6 to about 12 percent carboxy nitrile rubber, about 12 to 16 percent phenolic resin, and about 72 to about 82 percent friction modifiers, based on the total weight of cement solids.
  • the dispersion should contain a small but effective amount of a surfactant or dispersant to enhance wetting of the filaments by the solids.
  • the heat-curable cement system should also contain curing agents for the rubber and resin, and may also contain accelerators to reduce curing time.
  • Particulate friction modifiers for use in the cement system are well known and include carbon black, graphite, metal oxides, metallic powders, barytes, and the like.
  • the heat-curable cement system may contain well known organic fillers, an example of which is finely divided polymerized cashew nut oil.
  • the rovings from the second coating step generally will contain about 58 to 63 percent, preferably about 60 to about 62 percent, by weight of uncoated fibers, of cement solids, such amount being the cumulative total of both coating operations.
  • the rovings are dried to a moisture content on the order of about 2 to 4 percent by weight of coated filaments. When dried to this extent the rovings are somewhat tacky. As will be seen this property enhances the formation of the tape and clutch facing preforms formed thereof.
  • the rovings to which the heat-curable cement system has been applied and subsequently dried are combined to form a tape by gathering a plurality of rovings, e.g. 6 to 8, by rotating rollers or the like which twist the rovings together.
  • a plurality of rovings e.g. 6 to 8
  • rotating rollers or the like which twist the rovings together.
  • the resulting tape there will ordinarily be about 3 to 6 turns per linear foot.
  • the tape may be provided along its length with one or more helices of non-ferrous metal wire, e.g. brass, copper or lead wire, or of non-metallic material such as cotton, rayon or glass fiber yarn or thread.
  • non-ferrous metal wire e.g. brass, copper or lead wire
  • non-metallic material such as cotton, rayon or glass fiber yarn or thread.
  • the non-metallic helices can provide improved frictional properties, whereas the metal wire produces both improved friction and heat dissipation properties but, because of the additional weight, may reduce hot burst strength properties to some degree.
  • there is applied to the tape a plurality of helices of copper wire so that the total weight of wire is from about 10 to about 20 percent, by weight of coated tape.
  • the tape formed of continuous glass filaments and impregnated with the heat-curable cement system is wound in undulating fashion onto a revolving mandrel in such manner that the convolutions of the tape vary in the instantaneous radius at which they are being wound.
  • This arrangement is best illustrated in FIG. 2 of the drawings.
  • the resulting disc-shaped friction facing preform is then placed in a mold and heated at elevated temperatures in the range of about 350° to 375° F., under a pressure of about 3500 to 5000 psi for a short period of time, e.g. 2-3 minutes to consolidate and densify the preform and at least partially cure the binder.
  • the resulting facings are placed in an oven heated to a temperature of about 400° to 450° F. where they remain for several hours. During this latter heat treatment the resin is converted into the infusible, insoluble state and the rubber is vulcanized.
  • the clutch facings are then subject to conventional mechanical processing such as grinding to achieve acceptable tolerances, and drilled to provide holes by means of which the facings are attached to the power train of an internal combustion engine (see particularly FIGS. 3 and 4).
  • This example describes the preparation of clutch facings according to this invention.
  • glass fiber roving comprising about 2000 ends of continuous glass filaments having an average diameter of about 13 microns were used.
  • the surfaces of the filaments of the rovings had been chemically treated previously to render them capable of forming a strong bond with the pre-coat below described.
  • a number of the glass fiber roving were paid off a creel and passed through tensioning devices and ceramic guides to the coater. Each end of the roving prior to entering the coater was splayed so that the filaments would be wet with the pre-coat. Excess pre-coat was then removed.
  • the coating composition comprised an aqueous dispersion containing about 10 weight percent of the following solids and about 1 percent surfactant:
  • the rovings were dried by infra red means whereby sufficient water was removed to reduce the moisture content of the rovings to about 4%, by weight, based on the weight of the coated filaments.
  • the dried rovings which contained about 10 weight percent of pre-coat solids, were then passed to a roller coater in which there was an aqueous dispersion containing approximately 54 weight percent total of the following solids:
  • the impregnated rovings were passed through a tunnel drier where the moisture content thereof was again reduced to about 4 weight percent. This quantity of residual moisture imparts a tackiness to the filaments sufficient to render them pressure sensitive so that they adhere to one another.
  • the rovings contained about 61 percent of the above cement system, based on the weight of glass fibers.
  • a tape was formed by gathering the rovings by means of two pair of rotating rolls which twisted the rovings together to provide the resulting tape with about 3 twists per foot.
  • the tape was wound in undulating fashion to form a number of disc-shaped friction facing preforms which were placed in molds heated 360° F. where they were subjected to a pressure of 5000 psi for slightly more than 2 minutes to effect densification of the preform and partial cure of the cement system. Subsequently the clutch facings were further heated at 400-450° F. for about 51/2 hours to convert the resin into the infusible, insoluble state and to vulcanize the rubber. The clutch facings were ground to the following dimensions: O.D. 11 inches; I.D. 61/2 inches; thickness 0.137 inch.
  • Each clutch facing was riveted to the driven member making certain the rivets were properly tightened.
  • the mounted clutch facing was then heated for 15 minutes in a circulating air oven maintained at 500° F.
  • the mounted clutch facing was removed from the oven and promptly (within 15 seconds) mounted on the shaft of a Centrifugal Burst Machine.
  • the test was immediately begun and the driven member to which the test clutch facing was mounted reached 3500 rpm approximately 2 seconds. Thereafter the speed of the driven member was increased at an average rate of approximately 135 rpm/sec. until the clutch facing burst, at which time the speed of rotation was recorded.
  • the burst strength data obtained are set forth in Table I, below.
  • clutch facings were prepared using the material and procedures described in Example I.
  • the clutch facings had the following dimensions: O.D. 9 1/16 inches; I.D. 6 inches; thickness 0.125 inch.
  • the clutch facings were tested for burst strength using the procedure described in Example II. The results obtained are given in Table I, below:
  • a number of clutch facings were prepared using the materials and procedures described in Example I only with the following additional step.
  • An overlay of 18 percent copper wire was applied to the treated fiberglass tape by means of a braiding device for the purpose of improved heat dissipation.
  • the clutch facings had the following dimensions: O.D. 11 inches; I.D. 61/2 inches; thickness 0.137 inch.
  • the clutch facings were tested for burst strength using the procedure described in Example II. The results obtained are given in Table II below:

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  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Braking Arrangements (AREA)
  • Reinforced Plastic Materials (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)
  • Moulding By Coating Moulds (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
US05/819,760 1977-07-28 1977-07-28 Glass fiber friction facing Expired - Lifetime US4118528A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US05/819,760 US4118528A (en) 1977-07-28 1977-07-28 Glass fiber friction facing
CA306,621A CA1077868A (fr) 1977-07-28 1978-06-30 Garniture d'embrayage en fibre de verre
IT50408/78A IT1107786B (it) 1977-07-28 1978-07-20 Rivestimento di fibre di vetro per innesti a frizione e procedimento di produzione
SE7808041A SE425168B (sv) 1977-07-28 1978-07-21 Friktionsbelegg och forfarande att framstella detsamma
JP53090538A JPS5945005B2 (ja) 1977-07-28 1978-07-26 グラスフアイバ−製フリクシヨンフエ−シングおよびその製法
BE189524A BE869305A (fr) 1977-07-28 1978-07-27 Garniture de friction en fibres de verre
GB7831326A GB2002466B (en) 1977-07-28 1978-07-27 Glass fibre friction element
FR7822327A FR2398771A1 (fr) 1977-07-28 1978-07-27 Garniture de friction en fibres de verre et son procede de fabrication
DE2833289A DE2833289C2 (de) 1977-07-28 1978-07-28 Ringscheibenförmiger Reibbelag und Verfahren zu seiner Herstellung

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/819,760 US4118528A (en) 1977-07-28 1977-07-28 Glass fiber friction facing

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US4118528A true US4118528A (en) 1978-10-03

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US05/819,760 Expired - Lifetime US4118528A (en) 1977-07-28 1977-07-28 Glass fiber friction facing

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US (1) US4118528A (fr)
JP (1) JPS5945005B2 (fr)
BE (1) BE869305A (fr)
CA (1) CA1077868A (fr)
DE (1) DE2833289C2 (fr)
FR (1) FR2398771A1 (fr)
GB (1) GB2002466B (fr)
IT (1) IT1107786B (fr)
SE (1) SE425168B (fr)

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3023186A1 (de) * 1979-06-21 1981-01-08 Raybestos Manhattan Inc Reibmaterial, daraus hergestellte gegenstaende und verfahren zu ihrer herstellung
DE3023187A1 (de) * 1979-06-21 1981-01-08 Raybestos Manhattan Inc Reibteil, verfahren zu seiner herstellung und seine verwendung
DE3023188A1 (de) * 1979-06-21 1981-01-08 Raybestos Manhattan Inc Reibmaterial und daraus hergestellte gegenstaende
FR2489354A1 (fr) * 1980-08-29 1982-03-05 Borg Warner Materiau de friction exempt d'amiante
EP0063453A2 (fr) * 1981-04-10 1982-10-27 Ferodo Limited Garnitures de friction
US4372795A (en) * 1980-10-31 1983-02-08 Messerschmitt-Boelkow-Blohm Gesellschaft Mit Beschraenkter Haftung Method for the manufacture of a coupling or clutch element
US4384640A (en) * 1979-06-21 1983-05-24 Raymark Corporation Friction material for clutch facings and the like
FR2532244A1 (fr) * 1982-08-24 1984-03-02 Borg Warner Procede de preparation de garnitures d'embrayage a friction
FR2532243A1 (fr) * 1982-08-13 1984-03-02 Borg Warner Bande continue revetue par extrusion pour la fabrication de garnitures d'embrayage a friction
EP0183335A2 (fr) * 1984-11-29 1986-06-04 Fichtel & Sachs AG Elément de friction exempt d'amiante
JPS61293838A (ja) * 1985-06-21 1986-12-24 Aisin Chem Co Ltd クラツチ被動板の一体成形方法
US4656203A (en) * 1984-10-20 1987-04-07 Turner & Newall Plc Friction materials and their manufacture
US4663368A (en) * 1984-03-03 1987-05-05 Turner & Newall Plc Friction materials and their manufacture
DE3800231A1 (de) * 1987-01-08 1988-07-21 Akebono Brake Ind Verfahren zur herstellung eines verstaerkungselements fuer asbest-freie reibmaterialien
US4775705A (en) * 1984-10-20 1988-10-04 T&N Plc Friction materials and their manufacture
US5217778A (en) * 1982-10-21 1993-06-08 Raymark Industries, Inc. Composite fiber friction facing
FR2711754A1 (fr) * 1993-10-29 1995-05-05 Fichtel & Sachs Ag Garniture de friction pour un embrayage à friction de véhicule automobile.
US5494747A (en) * 1992-02-27 1996-02-27 G B Tools & Components Exports Limited Textile treatment
US5558738A (en) * 1992-10-09 1996-09-24 Rector; Horst D. Method for laying down threads
FR2759387A1 (fr) * 1997-02-12 1998-08-14 Carbone Ind Realisation de preforme fibreuse annulaire par enroulement de ruban
US5823314A (en) * 1993-12-15 1998-10-20 Nsk-Warner Kabushiki Kaisha Wet frictional engagement plate
EP0965770A1 (fr) * 1998-06-17 1999-12-22 Valeo Procédé de fabrication d'un matériau de friction et plus particulièrement d'une couronne de friction pour disque de friction d'embrayage et couronne d'embrayage
FR2792383A1 (fr) * 1999-04-16 2000-10-20 Valeo Procede de fabrication d'un materiau de friction et notamment d'une couronne de friction d'embrayage
US6419981B1 (en) 1998-03-03 2002-07-16 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
US6593255B1 (en) 1998-03-03 2003-07-15 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
FR2861443A1 (fr) * 2003-10-23 2005-04-29 Valeo Materiaux De Friction Garniture de frottement et procede de fabrication d'une telle garniture de frottement.
US6949289B1 (en) * 1998-03-03 2005-09-27 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
US20060172112A1 (en) * 2002-12-09 2006-08-03 Aisin Kako Kabushiki Kaisha Friction material and its manufacturing method
US7354641B2 (en) 2004-10-12 2008-04-08 Ppg Industries Ohio, Inc. Resin compatible yarn binder and uses thereof
EP2048406A3 (fr) * 2007-10-10 2009-06-10 Miba Frictec GmbH Procédé de fabrication d'une garniture de friction
US20100012449A1 (en) * 2007-04-02 2010-01-21 Luk Lamellen Und Kupplungsbau Beteiligungs Kg Friction lining
US20100080960A1 (en) * 2007-06-08 2010-04-01 Luk Lamellen Und Kupplungsbau Beteiligungs Kg Friction lining
CN101925754A (zh) * 2008-02-22 2010-12-22 瓦莱奥摩擦材料公司 摩擦材料尤其是离合器摩擦环的制造方法
US20110024257A1 (en) * 2008-04-07 2011-02-03 Schaeffler Technologies Gmbh & Co. Kg Friction lining for a friction clutch
US8062746B2 (en) 2003-03-10 2011-11-22 Ppg Industries, Inc. Resin compatible yarn binder and uses thereof
US8105690B2 (en) 1998-03-03 2012-01-31 Ppg Industries Ohio, Inc Fiber product coated with particles to adjust the friction of the coating and the interfilament bonding
CN104126079A (zh) * 2012-02-14 2014-10-29 大陆-特韦斯贸易合伙股份公司及两合公司 纤维复合材料制成的内通风的机动车制动盘

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JPH0425556A (ja) * 1990-05-21 1992-01-29 Daiwa Taika Renga Senzoushiyo:Kk 複合材料
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US4244994A (en) * 1979-06-21 1981-01-13 Raybestos-Manhattan, Inc. Laminated aramid fiber friction members
DE3023187A1 (de) * 1979-06-21 1981-01-08 Raybestos Manhattan Inc Reibteil, verfahren zu seiner herstellung und seine verwendung
US4320823A (en) * 1979-06-21 1982-03-23 Raybestos-Manhattan, Inc. Friction members formed from compositions containing aramid fibers and an aqueous heat-hardenable cement comprising a water soluble phenolic resin and a heat-curable elastomer
US4349595A (en) * 1979-06-21 1982-09-14 Raybestos-Manhattan, Inc. Friction material for clutch facings and the like
FR2489354A1 (fr) * 1980-08-29 1982-03-05 Borg Warner Materiau de friction exempt d'amiante
US4372795A (en) * 1980-10-31 1983-02-08 Messerschmitt-Boelkow-Blohm Gesellschaft Mit Beschraenkter Haftung Method for the manufacture of a coupling or clutch element
EP0063453A3 (en) * 1981-04-10 1982-11-24 Ferodo Limited Improvements in and relating to action linings
EP0063453A2 (fr) * 1981-04-10 1982-10-27 Ferodo Limited Garnitures de friction
FR2532243A1 (fr) * 1982-08-13 1984-03-02 Borg Warner Bande continue revetue par extrusion pour la fabrication de garnitures d'embrayage a friction
FR2532244A1 (fr) * 1982-08-24 1984-03-02 Borg Warner Procede de preparation de garnitures d'embrayage a friction
US5217778A (en) * 1982-10-21 1993-06-08 Raymark Industries, Inc. Composite fiber friction facing
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US4775705A (en) * 1984-10-20 1988-10-04 T&N Plc Friction materials and their manufacture
US4656203A (en) * 1984-10-20 1987-04-07 Turner & Newall Plc Friction materials and their manufacture
EP0183335A3 (en) * 1984-11-29 1987-07-08 Borg-Warner Corporation Asbestos free friction element
EP0183335A2 (fr) * 1984-11-29 1986-06-04 Fichtel & Sachs AG Elément de friction exempt d'amiante
JPS61293838A (ja) * 1985-06-21 1986-12-24 Aisin Chem Co Ltd クラツチ被動板の一体成形方法
JPH0559819B2 (fr) * 1985-06-21 1993-09-01 Aishin Kako Kk
DE3800231A1 (de) * 1987-01-08 1988-07-21 Akebono Brake Ind Verfahren zur herstellung eines verstaerkungselements fuer asbest-freie reibmaterialien
US4924566A (en) * 1987-01-08 1990-05-15 Akebono Brake Industry Co., Ltd. Method for manufacturing a reinforcing element for asbestos free friction material
US5494747A (en) * 1992-02-27 1996-02-27 G B Tools & Components Exports Limited Textile treatment
US5558738A (en) * 1992-10-09 1996-09-24 Rector; Horst D. Method for laying down threads
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FR2759387A1 (fr) * 1997-02-12 1998-08-14 Carbone Ind Realisation de preforme fibreuse annulaire par enroulement de ruban
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US6419981B1 (en) 1998-03-03 2002-07-16 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
US6593255B1 (en) 1998-03-03 2003-07-15 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
US6949289B1 (en) * 1998-03-03 2005-09-27 Ppg Industries Ohio, Inc. Impregnated glass fiber strands and products including the same
US8105690B2 (en) 1998-03-03 2012-01-31 Ppg Industries Ohio, Inc Fiber product coated with particles to adjust the friction of the coating and the interfilament bonding
FR2779989A1 (fr) * 1998-06-17 1999-12-24 Valeo Procede de fabrication d'un materiau de friction et plus particulierement d'une couronne de friction pour disque de friction d'embrayage et couronne d'embrayage
US6503613B1 (en) 1998-06-17 2003-01-07 Valeo Dry friction clutch liner crowns, and methods of making them
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EP0965770B2 (fr) † 1998-06-17 2009-06-17 Valeo Matériaux de Friction Procédé de fabrication d'un matériau de friction et plus particulièrement d'une couronne de friction pour disque de friction d'embrayage.
KR100630030B1 (ko) * 1998-06-17 2006-09-27 발레오 건식 마찰 클러치 라이너 크라운 및 그의 제조 방법
FR2792383A1 (fr) * 1999-04-16 2000-10-20 Valeo Procede de fabrication d'un materiau de friction et notamment d'une couronne de friction d'embrayage
WO2000063577A1 (fr) * 1999-04-16 2000-10-26 Valeo Procede de fabrication d'un materiau de friction et notamment d'une couronne de friction d'embrayage
US20110041412A1 (en) * 2002-12-09 2011-02-24 Aisin Kako Kabushiki Kaisha Friction material and its manufacturing method
US20060172112A1 (en) * 2002-12-09 2006-08-03 Aisin Kako Kabushiki Kaisha Friction material and its manufacturing method
US20060169403A1 (en) * 2002-12-09 2006-08-03 Aisin Kako Kabushiki Kaisha Friction material and its manufacturing method
US7972675B2 (en) 2002-12-09 2011-07-05 Aisin Kako Kabushiki Kaisha Friction material
US7488440B2 (en) * 2002-12-09 2009-02-10 Aisin Kako Kabushiki Kaisha Friction material and its manufacturing method
US20090136662A1 (en) * 2002-12-09 2009-05-28 Aisin Kako Kabushiki Kaisha Friction material and its manufacturing method
US8062746B2 (en) 2003-03-10 2011-11-22 Ppg Industries, Inc. Resin compatible yarn binder and uses thereof
FR2861443A1 (fr) * 2003-10-23 2005-04-29 Valeo Materiaux De Friction Garniture de frottement et procede de fabrication d'une telle garniture de frottement.
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CN104126079A (zh) * 2012-02-14 2014-10-29 大陆-特韦斯贸易合伙股份公司及两合公司 纤维复合材料制成的内通风的机动车制动盘
US20150014104A1 (en) * 2012-02-14 2015-01-15 Continental Teves & AG & Co. oHG Internally ventilated motor vehicle brake disc made of fibre composite material
US9255618B2 (en) * 2012-02-14 2016-02-09 Continental Teves Ag & Co. Ohg Internally ventilated motor vehicle brake disc made of fibre composite material

Also Published As

Publication number Publication date
IT7850408A0 (it) 1978-07-20
JPS5425975A (en) 1979-02-27
FR2398771A1 (fr) 1979-02-23
FR2398771B1 (fr) 1983-10-14
JPS5945005B2 (ja) 1984-11-02
IT1107786B (it) 1985-11-25
GB2002466B (en) 1982-02-17
CA1077868A (fr) 1980-05-20
SE7808041L (sv) 1979-01-29
GB2002466A (en) 1979-02-21
BE869305A (fr) 1978-11-16
SE425168B (sv) 1982-09-06
DE2833289A1 (de) 1979-02-08
DE2833289C2 (de) 1987-03-26

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